FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

1231150005: Isolated hypoplasia of fovea centralis (disorder)


Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5071675017 Isolated hypoplasia of fovea centralis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5071676016 Isolated foveal hypoplasia en Synonym Active Case insensitive SNOMED CT core
5071677013 Isolated hypoplasia of fovea centralis en Synonym Active Case insensitive SNOMED CT core
5071678015 A rare macular disorder with characteristics mostly of a variable degree of decreased visual acuity, jerk or pendular nystagmus and typical ocular findings at imaging. The disease is usually bilateral. Rarely nystagmus can be absent. Locally the disease has characteristics of an underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone and persistence of inner retinal layers at the fovea in absence of concomitant ocular or systemic pathology. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated foveal hypoplasia Is a Anomaly of eye true Inferred relationship Some
Isolated foveal hypoplasia Is a Disorder of macula of retina true Inferred relationship Some
Isolated foveal hypoplasia Is a Developmental disorder true Inferred relationship Some
Isolated foveal hypoplasia Finding site Structure of fovea centralis true Inferred relationship Some 1
Isolated foveal hypoplasia Associated morphology Hypoplasia true Inferred relationship Some 1
Isolated foveal hypoplasia Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start